Rapid tissue prototyping with micro-organospheres.

dc.contributor.author

Wang, Zhaohui

dc.contributor.author

Boretto, Matteo

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Millen, Rosemary

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Natesh, Naveen

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Reckzeh, Elena S

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Hsu, Carolyn

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Negrete, Marcos

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Yao, Haipei

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Quayle, William

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Heaton, Brook E

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Harding, Alfred T

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Bose, Shree

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Driehuis, Else

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Beumer, Joep

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Rivera, Grecia O

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van Ineveld, Ravian L

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Gex, Donald

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DeVilla, Jessica

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Wang, Daisong

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Puschhof, Jens

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Geurts, Maarten H

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Yeung, Athena

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Hamele, Cait

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Smith, Amber

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Bankaitis, Eric

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Xiang, Kun

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Ding, Shengli

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Nelson, Daniel

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Delubac, Daniel

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Rios, Anne

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Abi-Hachem, Ralph

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Jang, David

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Goldstein, Bradley J

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Glass, Carolyn

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Heaton, Nicholas S

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Hsu, David

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Clevers, Hans

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Shen, Xiling

dc.date.accessioned

2022-12-30T03:07:48Z

dc.date.available

2022-12-30T03:07:48Z

dc.date.issued

2022-09

dc.date.updated

2022-12-30T03:07:43Z

dc.description.abstract

In vitro tissue models hold great promise for modeling diseases and drug responses. Here, we used emulsion microfluidics to form micro-organospheres (MOSs), which are droplet-encapsulated miniature three-dimensional (3D) tissue models that can be established rapidly from patient tissues or cells. MOSs retain key biological features and responses to chemo-, targeted, and radiation therapies compared with organoids. The small size and large surface-to-volume ratio of MOSs enable various applications including quantitative assessment of nutrient dependence, pathogen-host interaction for anti-viral drug screening, and a rapid potency assay for chimeric antigen receptor (CAR)-T therapy. An automated MOS imaging pipeline combined with machine learning overcomes plating variation, distinguishes tumorspheres from stroma, differentiates cytostatic versus cytotoxic drug effects, and captures resistant clones and heterogeneity in drug response. This pipeline is capable of robust assessments of drug response at individual-tumorsphere resolution and provides a rapid and high-throughput therapeutic profiling platform for precision medicine.

dc.identifier

S2213-6711(22)00376-9

dc.identifier.issn

2213-6711

dc.identifier.issn

2213-6711

dc.identifier.uri

https://hdl.handle.net/10161/26393

dc.language

eng

dc.publisher

Elsevier BV

dc.relation.ispartof

Stem cell reports

dc.relation.isversionof

10.1016/j.stemcr.2022.07.016

dc.subject

Organoids

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Humans

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Antineoplastic Agents

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Drug Evaluation, Preclinical

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Microfluidics

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Precision Medicine

dc.title

Rapid tissue prototyping with micro-organospheres.

dc.type

Journal article

duke.contributor.orcid

Glass, Carolyn|0000-0002-8850-9906

duke.contributor.orcid

Shen, Xiling|0000-0002-4978-3531

pubs.begin-page

1959

pubs.end-page

1975

pubs.issue

9

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Basic Science Departments

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Clinical Science Departments

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Cell Biology

pubs.organisational-group

Molecular Genetics and Microbiology

pubs.organisational-group

Pathology

pubs.organisational-group

Duke Cancer Institute

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Duke Human Vaccine Institute

pubs.organisational-group

Neurosurgery

pubs.organisational-group

Head and Neck Surgery & Communication Sciences

pubs.publication-status

Published

pubs.volume

17

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